2-Pentanone → HCID 21879870, compound
Reaction equation
CC(N)COCC(OCC(OCC([NH2:16])C)C)C.[C:18]([O-:23])(=[O:22])[C:19]([CH3:21])=[CH2:20].C([C:27]([CH3:29])=O)CC>>[NH2:16][C:18]([O:23][CH2:27][CH3:29])=[O:22].[C:18]([O-:23])(=[O:22])[C:19]([CH3:21])=[CH2:20]Participants
4
Procedure
59.95 g-(0.010 m) α,β-di(1-methyl-aminoethyl) poly-(ethylene oxide-co-propyleneoxide) of MW 5995 (Jeffamine-ED 5000, TEXACO Corp.) and 59.95 g of anhydrous methyl propyl ketone are charged into a 3-necked round bottomed flask equipped with a stirrer, nitrogen inlet, condenser, thermometer and dropping funnel. The solution is stirred at room temperature under dry nitrogen. Then 3.10 g (0.020 mole) of 2-isocyanotoethyl methacrylate (MW 155) dissolved in 3.1 g of anhydrous methyl propyl ketone are added slowly from the dropping funnel. The mildly exothermic reaction is maintained at 35° C. and below by water bath cooling for 1 hour at which time an IR analysis shows the reaction to be complete.
Workup
- customequipped with a stirrer, nitrogen inlet, condenser
- additionare added slowly from the dropping funnel
- customThe mildly exothermic reaction
- temperatureis maintained at 35° C. and below by water bath
- temperaturecooling for 1 hour at which time an IR analysis
- customthe reaction
Sources & evidence
- ORD record
- ord-f115200f1b6544c8b249c942d63f2aba
- Source dataset
- uspto-grants-1994_08
- Patent number
- US05334681
Reaction notes
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